Key result
Oral estrogen significantly reduced mean IGF-I levels, postprandial lipid oxidation, and protein synthesis compared with transdermal estrogen in growth hormone-deficient women (P<0.05).
Why the study?
Does oral estrogen antagonize the metabolic actions of growth hormone compared to transdermal estrogen in growth hormone-deficient women?
RCT (n=8)
Crossover
Does oral estrogen antagonize the metabolic actions of growth hormone compared to transdermal estrogen in growth hormone-deficient women?
p-value: p=<0.05
Oral estrogen antagonizes the metabolic actions of growth hormone in growth hormone-deficient women, suggesting estrogen replacement should be administered via a nonoral route in this population.
Transdermal estrogen preferred over oral in growth hormone-deficient women; extends evidence for route-dependent antagonism of growth hormone actions.
We have determined whether oral estrogen reduces the biological effects of growth hormone (GH) in GH-deficient (GHD) women compared with transdermal estrogen treatment. In two separate studies, eight GHD women randomly received either oral or transdermal estrogen for 8 wk before crossing over to the alternate route of administration. The first study assessed the effects of incremental doses of GH (0.5, 1.0, 2.0 IU/day for 1 wk each) on insulin-like growth factor I (IGF-I) levels during each estrogen treatment phase. The second study assessed the effects of GH (2 IU/day) on lipid oxidation and on protein metabolism using the whole body leucine turnover technique. Mean IGF-I level was significantly lower during oral estrogen treatment (P < 0.05) and rose dose dependently during GH administration by a lesser magnitude (P < 0.05) compared with transdermal treatment. Postprandial lipid oxidation was significantly lower with oral estrogen treatment, both before (P < 0.05) and during (P < 0.05) GH administration, compared with transdermal treatment. Protein synthesis was lower during oral estrogen both before and during GH administration (P < 0.05). Oral estrogen antagonizes several of the metabolic actions of GH. It may aggravate body composition abnormalities already present in GHD women and attenuate the beneficial effects of GH therapy. Estrogen replacement in GHD women should be administered by a nonoral route.
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Wolthers et al. (2001) conducted an RCT in Growth hormone deficiency (n=8). Oral estrogen vs. Transdermal estrogen was evaluated on IGF-I levels, lipid oxidation, and protein synthesis (p=<0.05). Oral estrogen significantly reduced mean IGF-I levels, postprandial lipid oxidation, and protein synthesis compared with transdermal estrogen in growth hormone-deficient women (P<0.05).
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